Sodium Bicarbonate
- Product NDC
- 0409-4916
- 11-digit product format
- 004094916
- Labeler code
- 0409
- Product ID
- 0409-4916_6404d8a8-4b75-4c19-8085-d5892343925e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM BICARBONATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hospira, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2006-02-16
- Marketing end
- 2022-02-01
- Substance
- SODIUM BICARBONATE
- Active strength
- 75 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0409-4916-14 | Sodium Bicarbonate | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | | 8 |
| 0409-4916-14 | Sodium Bicarbonate | 10 in 1 PACKAGE | INJECTION, SOLUTION | 10 | | 8 |
| 0409-4916-24 | Sodium Bicarbonate | 50 mL in 1 SYRINGE | INJECTION, SOLUTION | 50 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0409-4916 | SODIUM BICARBONATE INJECTION, SOLUTION [HOSPIRA, INC.] | 7 | Legacy NDC, 3 package rows | 20241220_ea20a5eb-641e-48cd-bcfa-74c04c45dfda.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0409-4916-14 | 00409491614 | 10 CARTON in 1 PACKAGE (0409-4916-14) > 1 SYRINGE in 1 CARTON > 50 mL in 1 SYRINGE (0409-4916-24) | 10 carton | 2020-07-23 | 0000-00-00 | No | No | Current |
| 0409-4916-24 | 00409491624 | 50 mL in 1 SYRINGE | 50 ml | | | | | Historical |
| 0409-4916-34 | 00409491634 | 10 CARTON in 1 PACKAGE (0409-4916-34) > 1 SYRINGE in 1 CARTON > 50 mL in 1 SYRINGE | 10 carton | 2006-02-16 | 0000-00-00 | No | No | Current |